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Noonan syndrome in diverse populations.

Paul S KruszkaAntonio R PorrasYonit A AddissieAngélica MorescoSofia MedranoGary T K MokGordon K C LeungCedrik Tekendo-NgongangAnnette UwinezaMeow-Keong ThongPremala MuthukumarasamyEngela HoneyEkanem N EkureOgochukwu J SokunbiNnenna KaluKelly L JonesJulie D KaplanOmar A Abdul-RahmanLisa M VincentAmber LoveKhadija BelhassanKarim OuldimIhssane El BouchikhiAnju ShuklaKatta M GirishaSiddaramappa Jagdish PatilNirmala D SirisenaVajira H W DissanayakeC Sampath PaththinigeRupesh MishraEva Klein-ZighelboimBertha E Gallardo JugoMiguel Chávez PastorHugo Hernán Abarca BarrigaSteven A SkinnerEloise J PrijolesEben BadoeAshleigh D GillVorasuk ShotelersukPatroula SmpokouMonisha S KislingCarlos R FerreiraLeon MutesaAndre MegarbaneAntonie D KlineAmy KimballEmmy OkelloPeter LwabiTwalib AlikuEmmanuel TenywaNonglak BoonchooduangPranoot TanpaiboonAntonio Richieri-CostaAmbroise WonkamBrian H Y ChungRoger E StevensonMarshall SummarKausik MandalShubha R PhadkeMaría G ObregonMarius G LinguraruMaximilian Muenke
Published in: American journal of medical genetics. Part A (2017)
Noonan syndrome (NS) is a common genetic syndrome associated with gain of function variants in genes in the Ras/MAPK pathway. The phenotype of NS has been well characterized in populations of European descent with less attention given to other groups. In this study, individuals from diverse populations with NS were evaluated clinically and by facial analysis technology. Clinical data and images from 125 individuals with NS were obtained from 20 countries with an average age of 8 years and female composition of 46%. Individuals were grouped into categories of African descent (African), Asian, Latin American, and additional/other. Across these different population groups, NS was phenotypically similar with only 2 of 21 clinical elements showing a statistically significant difference. The most common clinical characteristics found in all population groups included widely spaced eyes and low-set ears in 80% or greater of participants, short stature in more than 70%, and pulmonary stenosis in roughly half of study individuals. Using facial analysis technology, we compared 161 Caucasian, African, Asian, and Latin American individuals with NS with 161 gender and age matched controls and found that sensitivity was equal to or greater than 94% for all groups, and specificity was equal to or greater than 90%. In summary, we present consistent clinical findings from global populations with NS and additionally demonstrate how facial analysis technology can support clinicians in making accurate NS diagnoses. This work will assist in earlier detection and in increasing recognition of NS throughout the world.
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